A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035842



Internal ID19125061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56325080..56390374hg38UCSC Ensembl
Innerchr10:58084841..58150135hg19UCSC Ensembl
Innerchr10:57754847..57820141hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3865295
hg1965295
hg1865295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706926
Samples
Known GenesZWINT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035842
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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