A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724531



Internal ID18676126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36261761..36356920hg38UCSC Ensembl
Innerchr19:36752663..36847822hg19UCSC Ensembl
Innerchr19:41444503..41539662hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3895160
hg1995160
hg1895160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057579
Supporting Variants
Samples
Known GenesLINC00665, LOC100134317, ZFP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724531
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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