A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585677



Internal ID18883958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214486070..214546803hg38UCSC Ensembl
Innerchr2:215350794..215411527hg19UCSC Ensembl
Innerchr2:215059039..215119772hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3860734
hg1960734
hg1860734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007833
Supporting Variants
Samples
Known GenesVWC2L, VWC2L-IT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585677
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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