A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515824



Internal ID15096431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74163688..74699911hg38UCSC Ensembl
Innerchr10:75923446..76459669hg19UCSC Ensembl
Innerchr10:75593452..76129675hg18UCSC Ensembl
Innerchr10:75593452..76129675hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38536224
hg19536224
hg18536224
hg17536224
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697596, nssv685614, nssv678770, nssv678982, nssv692774, nssv664889, nssv705859, nssv695800, nssv706095, nssv693893, nssv698293, nssv671658
Samples
Known GenesADK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515824
Frequency
Sample Size2026
Observed Gain1
Observed Loss11
Observed Complex0
Frequencyn/a


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