A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517031



Internal ID15444324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6194574..6233230hg38UCSC Ensembl
Innerchr17:6097894..6136550hg19UCSC Ensembl
Innerchr17:6038618..6077274hg18UCSC Ensembl
Innerchr17:6038618..6077274hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3838657
hg1938657
hg1838657
hg1738657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653052, nssv653646, nssv693959, nssv686598, nssv669240, nssv659964, nssv673898, nssv686707, nssv666342, nssv652895, nssv684021, nssv660273, nssv667679, nssv666434, nssv654643, nssv663357, nssv680628, nssv658714, nssv684439, nssv658453, nssv675020, nssv677574, nssv683448, nssv673025, nssv658250, nssv665413, nssv661322, nssv664080, nssv671624, nssv689504, nssv675168, nssv666922, nssv688931, nssv681191, nssv653189, nssv685093, nssv676079, nssv671396, nssv663887, nssv681079, nssv673787
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517031
Frequency
Sample Size2026
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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