A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517423



Internal ID15098030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33777656..34498242hg38UCSC Ensembl
Innerchr17:32104675..32825261hg19UCSC Ensembl
Innerchr17:29128788..29849374hg18UCSC Ensembl
Innerchr17:29128788..29849374hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38720587
hg19720587
hg18720587
hg17720587
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696846, nssv660015, nssv681994, nssv679296, nssv655808, nssv665223, nssv680227, nssv696217, nssv703026, nssv664310, nssv660932, nssv655664, nssv657841, nssv651980
Samples
Known GenesASIC2, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517423
Frequency
Sample Size2026
Observed Gain2
Observed Loss12
Observed Complex0
Frequencyn/a


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