A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515872



Internal ID15442929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78582226..78663045hg38UCSC Ensembl
Innerchr17:76578308..76659127hg19UCSC Ensembl
Innerchr17:74089903..74170722hg18UCSC Ensembl
Innerchr17:74089903..74170722hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3880820
hg1980820
hg1880820
hg1780820
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677528, nssv659984, nssv687580, nssv665097, nssv690344, nssv676658, nssv704461, nssv669338, nssv666236
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515872
Frequency
Sample Size2026
Observed Gain6
Observed Loss3
Observed Complex0
Frequencyn/a


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