A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528802



Internal ID20902163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37602649..38484499hg38UCSC Ensembl
chr19:38093550..38975139hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38881851
hg19881590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198084
Samples
Known GenesC19orf33, CATSPERG, DPF1, FAM98C, GGN, KCNK6, LOC100631378, LOC644554, PPP1R14A, PSMD8, RASGRP4, RYR1, SIPA1L3, SPINT2, SPRED3, WDR87, YIF1B, ZFP30, ZNF540, ZNF573, ZNF607, ZNF781
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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