A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516703



Internal ID15443996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113841173..113896396hg38UCSC Ensembl
Innerchr3:113560020..113615243hg19UCSC Ensembl
Innerchr3:115042710..115097933hg18UCSC Ensembl
Innerchr3:115042710..115097933hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3855224
hg1955224
hg1855224
hg1755224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673752, nssv684261, nssv670271, nssv671613
Samples
Known GenesGRAMD1C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516703
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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