A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526734



Internal ID15107341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44963037..44996606hg38UCSC Ensembl
Innerchr10:45458485..45492054hg19UCSC Ensembl
Innerchr10:44778491..44812060hg18UCSC Ensembl
Innerchr10:44778491..44812060hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3833570
hg1933570
hg1833570
hg1733570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703077
Samples
Known GenesC10orf10, RASSF4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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